Corneal Manifestations of Metabolic Disease

Author:

Syed Zeba A.,Meghpara Beeran B.,Hammersmith Kristin M.,Rapuano Christopher J.

Publisher

Springer International Publishing

Reference205 articles.

1. Burns RP. Tyrosinemia. In: Gold DH, Weingeist TA, editors. The eye in systemic disease. Philadelphia: JB Lippincott; 1990. p. 327–9.

2. Macsai MS, Schwartz TL, Hinkle D, Hummel MB, Mulhern MG, Rootman D. Tyrosinemia type II: nine cases of ocular signs and symptoms. Am J Ophthalmol. 2001;132:522–7.

3. Buist NRM, Kennaway N, Fellman JG. Tyrosinemia type II: hepatic cytosol tyrosine amino-transferase deficiency. In: Bickel H, Wachtel U, editors. Inherited diseases of amino acid metabolism. Stuttgart: George Thieme; 1985. p. 203–35.

4. Grenier A, Lescault A, Laberge C, Gagne R, Mamer O. Detection of succinylacetone and the use of its measurement in mass screening for hereditary tyrosinemia. Clin Chim Acta. 1982;123:93–9.

5. Fuerst D. Tyrosinemia in mink. In: Tabbara KF, Cello RM, editors. Animal models of ocular disease. Springfield, IL: Charles C Thomas; 1984. p. 207–13.

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